Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Alias:
Classic 21-Ohd Cah
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency, also known as classic 21-ohd cah, is related to adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency and lipoid congenital adrenal hyperplasia. An important gene associated with Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency is CYP21A2 (Cytochrome P450 Family 21 Subfamily A Member 2). The drugs Racepinephrine and Immunoglobulins have been mentioned in the context of this disorder. Affiliated tissues include uterus and bone, and related phenotypes are increased circulating androgen concentration and decreased circulating cortisol level
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
1-9/100000
2
8
116

Medical Symptom

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Description
HPO Frequency
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HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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MGI
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Publications
No data available

References Literature

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